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Polymorphism and protein expression of MUTYH gene for risk of rheumatoid arthritis.
Chen, Shih-Yin; Chen, Hsin-Han; Huang, Yu-Chuen; Liu, Shih-Ping; Lin, Ying-Ju; Lo, Sui-Foon; Chang, Yuan-Yen; Lin, Hui-Wen; Huang, Chung-Ming; Tsai, Fuu-Jen.
Afiliação
  • Chen SY; School of Chinese Medicine, China Medical University, Taichung, 404, Taiwan.
  • Chen HH; Genetics Center, Department of Medical Research, China Medical University Hospital, Taichung, 404, Taiwan.
  • Huang YC; Division of Plastic and Reconstructive Surgery, China Medical University Hospital, Taichung, 404, Taiwan.
  • Liu SP; School of Chinese Medicine, China Medical University, Taichung, 404, Taiwan.
  • Lin YJ; Genetics Center, Department of Medical Research, China Medical University Hospital, Taichung, 404, Taiwan.
  • Lo SF; Center for Neuropsychiatry, China Medical University Hospital, Taichung, 404, Taiwan.
  • Chang YY; School of Chinese Medicine, China Medical University, Taichung, 404, Taiwan.
  • Lin HW; Genetics Center, Department of Medical Research, China Medical University Hospital, Taichung, 404, Taiwan.
  • Huang CM; Department of Physical Medicine and Rehabilitation, China Medical University Hospital, Taichung, 404, Taiwan.
  • Tsai FJ; Department of Microbiology and Immunology, and Institute of Microbiology and Immunology, School of Medicine, Chung Shan Medical University, Taichung, Taiwan.
BMC Musculoskelet Disord ; 18(1): 69, 2017 02 07.
Article em En | MEDLINE | ID: mdl-28173856
BACKGROUND: We have previously described the association between rheumatoid arthritis (RA) prevalence and the two mutY Homolog (E. coli) (MUTYH) SNPs (rs3219463 and rs3219476) among the Taiwanese population. This present study will aim to elucidate whether the SNPs can alter the expression of EGFR in the progression of RA. METHODS: The cohort study included 368 Taiwan's Han Chinese RA patients and 364 healthy controls. Blood samples collected from the participants were analyzed to determine their serum MUTYH levels and to identify rs3219463 SNP of MUTYH from their genomic DNA. RESULTS: Our data resulted in a statistically significant difference in genotype frequency distributions at rs3219463 for RA patients and controls (p < 0.0002). Also, the patients with G carrier at rs3219463 were less likely to suffer from painful joints (p < 0.006) and DAS28 scores (p < 0.003). Furthermore, the increase in serum level of MUTYH was also observed in RA patients (p < 0.005). CONCLUSIONS: Our study showed that RA is associated with rs3219463 SNP in EGFR gene and an increased serum level of the MUTYH protein. These findings suggest MUTYH is worthy of further investigation as a therapeutic target for RA.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Artrite Reumatoide / Predisposição Genética para Doença / Polimorfismo de Nucleotídeo Único / DNA Glicosilases Tipo de estudo: Etiology_studies / Incidence_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Female / Humans / Male Idioma: En Ano de publicação: 2017 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Artrite Reumatoide / Predisposição Genética para Doença / Polimorfismo de Nucleotídeo Único / DNA Glicosilases Tipo de estudo: Etiology_studies / Incidence_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Female / Humans / Male Idioma: En Ano de publicação: 2017 Tipo de documento: Article